Canonical Allele Identifier: CA2610079691

Gene: FAS

Linked Data

• gnomAD v4: 10-89014543-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014543T>C , CM000672.2:g.89014543T>C	GRCh38
NC_000010.10:g.90774300T>C , CM000672.1:g.90774300T>C	GRCh37
NC_000010.9:g.90764280T>C	NCBI36
NG_009089.2:g.29013T>C , LRG_134:g.29013T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1410T>C
ENST00000355740.8:c.*424T>C	ENSP00000347979.3:n.*424T>C
ENST00000357339.7:c.*93T>C	ENSP00000349896.2:n.*93T>C
ENST00000371857.8:n.2646T>C
ENST00000460510.6:c.*93T>C	ENSP00000512812.1:n.*93T>C
ENST00000466081.6:n.2750T>C
ENST00000477270.6:c.*93T>C	ENSP00000512813.1:n.*93T>C
ENST00000479522.6:c.*530T>C	ENSP00000424113.1:n.*530T>C
ENST00000484444.6:c.*542T>C	ENSP00000420975.1:n.*542T>C
ENST00000488877.6:c.992T>C	ENSP00000425159.1:n.992T>C
ENST00000492756.7:c.*530T>C	ENSP00000422453.1:n.*530T>C
ENST00000494799.6:c.*93T>C	ENSP00000512834.1:n.*93T>C
ENST00000562983.3:c.*93T>C	ENSP00000512845.1:n.*93T>C
ENST00000612663.6:c.*503T>C	ENSP00000477997.3:n.*503T>C
ENST00000640140.2:n.1246T>C
ENST00000640250.2:n.600T>C
ENST00000640681.2:n.1205T>C
ENST00000696723.1:n.4734T>C
ENST00000696741.1:n.2739T>C
ENST00000696742.1:n.2466T>C
ENST00000696743.1:n.3869T>C
ENST00000696744.1:n.1140T>C
ENST00000696767.1:n.1435T>C
ENST00000696768.1:c.*424T>C	ENSP00000512859.1:n.*424T>C
ENST00000696769.1:n.2790T>C
ENST00000696771.1:c.*93T>C	ENSP00000512860.1:n.*93T>C
ENST00000696772.1:n.2704T>C
ENST00000696773.1:n.2443T>C
ENST00000696774.1:n.6211T>C
ENST00000696776.1:c.*93T>C	ENSP00000512861.1:n.*93T>C
ENST00000696777.1:n.2509T>C
ENST00000696778.1:n.1537T>C
ENST00000696779.1:c.*93T>C	ENSP00000512862.1:n.*93T>C
ENST00000696780.1:c.*93T>C	ENSP00000512863.1:n.*93T>C
ENST00000696781.1:c.*93T>C	ENSP00000512864.1:n.*93T>C
ENST00000696782.1:c.*503T>C	ENSP00000512865.1:n.*503T>C
ENST00000696783.1:n.2969T>C
ENST00000696992.1:n.2218T>C
ENST00000696995.1:n.4630T>C
ENST00000696996.1:n.2543T>C
ENST00000696997.1:c.*731T>C	ENSP00000513028.1:n.*731T>C
ENST00000696998.1:n.2355T>C
ENST00000696999.1:c.*93T>C	ENSP00000513029.1:n.*93T>C
ENST00000697036.1:c.*517T>C	ENSP00000513060.1:n.*517T>C
ENST00000697037.1:n.1136T>C
ENST00000697093.1:n.3337T>C
ENST00000697094.1:n.3684T>C
ENST00000697095.1:c.*2302T>C	ENSP00000513104.1:n.*2302T>C
ENST00000697096.1:n.2234T>C
ENST00000697097.1:c.*93T>C	ENSP00000513105.1:n.*93T>C
ENST00000562983.2:n.1287T>C
ENST00000690268.1:c.*93T>C	ENSP00000509810.1:n.*93T>C
ENST00000355740.7:c.*427T>C	ENSP00000347979.3:n.*427T>C
ENST00000640140.1:n.1273T>C
ENST00000640250.1:n.600T>C
ENST00000640681.1:n.1222T>C
ENST00000652046.1:c.*93T>C MANE Select	ENSP00000498466.1:n.*93T>C
ENST00000352159.8:c.*418T>C	ENSP00000345601.4:n.*418T>C
ENST00000355740.6:c.*93T>C	ENSP00000347979.2:n.*93T>C
ENST00000479522.5:c.*530T>C	ENSP00000424113.1:n.*530T>C
ENST00000484444.5:c.*542T>C	ENSP00000420975.1:n.*542T>C
ENST00000494410.5:c.*459T>C	ENSP00000423755.1:n.*459T>C
NM_000043.4:c.*93T>C , LRG_134t1:c.*93T>C	NP_000034.1:n.*93T>C
NM_152871.2:c.*93T>C	NP_690610.1:n.*93T>C
NM_152872.2:c.*413T>C	NP_690611.1:n.*413T>C
NR_028033.2:n.1275T>C
NR_028034.2:n.1137T>C
NR_028035.2:n.1200T>C
NR_028036.2:n.1338T>C
XM_006717819.2:c.*93T>C	XP_006717882.1:n.*93T>C
XM_011539764.1:c.*93T>C	XP_011538066.1:n.*93T>C
XM_011539765.1:c.*93T>C	XP_011538067.1:n.*93T>C
XM_011539766.1:c.*93T>C	XP_011538068.1:n.*93T>C
XM_011539767.1:c.*93T>C	XP_011538069.1:n.*93T>C
NM_000043.5:c.*93T>C	NP_000034.1:n.*93T>C
NM_001320619.1:c.*424T>C	NP_001307548.1:n.*424T>C
NM_152871.3:c.*93T>C	NP_690610.1:n.*93T>C
NM_152872.3:c.*413T>C	NP_690611.1:n.*413T>C
NR_028033.3:n.1247T>C
NR_028034.3:n.1109T>C
NR_028035.3:n.1172T>C
NR_028036.3:n.1310T>C
NR_135313.1:n.1227T>C
NR_135314.1:n.1410T>C
NR_135315.1:n.1163T>C
XM_006717819.3:c.*93T>C	XP_006717882.1:n.*93T>C
XM_011539764.2:c.*93T>C	XP_011538066.1:n.*93T>C
XM_011539765.2:c.*93T>C	XP_011538067.1:n.*93T>C
XM_011539766.2:c.*93T>C	XP_011538068.1:n.*93T>C
XM_011539767.3:c.*93T>C	XP_011538069.1:n.*93T>C
XR_945732.3:n.1169T>C
XR_945733.2:n.1106T>C
NM_000043.6:c.*93T>C MANE Select	NP_000034.1:n.*93T>C
NM_001320619.2:c.*424T>C	NP_001307548.1:n.*424T>C
NM_152871.4:c.*93T>C	NP_690610.1:n.*93T>C
NM_152872.4:c.*413T>C	NP_690611.1:n.*413T>C
NR_028033.4:n.1008T>C
NR_028034.4:n.870T>C
NR_028035.4:n.933T>C
NR_028036.4:n.1071T>C
NR_135313.2:n.988T>C
NR_135314.2:n.1267T>C
NR_135315.2:n.1020T>C